Anthrax Investigation Guideline - Kansas Department of Health - kdheks 2025

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Cultures of -hemolytic, nonmotile, catalase positive, and gram-positive rods are considered as presumptive B. anthracis and sent to a CDC Laboratory Response Network (LRN) reference laboratory for confirmatory testing and further characterization.
The current gold standard for diagnosis of inhalational anthrax is the blood culture, which requires 24 h to a negative culture and 3 to 4 days to confirm positive cases (5).
The Bacillus anthracis ELISA Kit is an immunoassay for the detection and identification of Bacillus anthracis, the causative agent of anthrax. The assay can detect vegetative cells and spores. The kit is intended for laboratory analysis and quantification of B. anthracis contained in environmental samples.
Anthrax in people is a reportable condition in all states and territories and is a nationally notifiable condition. CDC and health departments use a standardized case definition to track anthrax in the United States. CDC publishes weekly and annual surveillance data in the Notifiable Infectious Disease Data Tables.
A sample of fluid from a suspicious lesion on your skin or a small tissue sample (biopsy) may be tested in a lab for signs of cutaneous anthrax. Blood tests. You may have a small amount of blood drawn thats checked in a lab for anthrax bacteria. Chest X-ray or computerized tomography (CT) scan.
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Conventional methods of B. anthracis identification include growth on selective media, lack of hemolysis, lack of motility, capsule staining, gamma phage lysis, String-of-pearls reaction, and susceptibility to penicillin.

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